MedicalDevice_TLB_8.25

Good Laboratory Practice Testing (GLP)

Available from Surpass Inc.

With hundreds of GLP-compliant studies completed for medical devices and therapies, Surpass has earned an international reputation as a preclinical laboratory you can trust. Our GLP quality system addresses 21 CFR Part 58 and 21 CFR Part 11 requirements and provides experienced study directors and quality assurance specialists to assist with individual study needs. We have successfully completed multiple FDA inspections. Contact Surpass today to discuss your upcoming GLP project.

Rate and Review Surpass Inc.

Rating: 0 - 0 reviews
Let users know what you would have wanted to know about this company.
Click on a star to rate this company
 
  Privacy Policy.
When writing a review, please adhere to the Review Guidelines.